Our purpose is to bring hope to life by enabling life-changing therapies for patients around the globe, creating a healthier and happier tomorrow. Our mission is to work side by side with our customers in order to improve patients’ lives by bringing new biopharmaceuticals to market.
At AGC Biologics in Søborg, manufacturing is where innovation becomes real treatments for patients worldwide. Our downstream production teams play a key role in this journey by purifying biologic products and preparing the critical solutions that enable safe and reliable production.
As a Technician/ Senior Technician in Downstream/ Buffer Preparation, you will become part of our SYD22 facility, a modern production area currently in ramp-up mode. Here, you will work hands-on with advanced manufacturing processes that support preclinical, clinical, and commercial production for international biotech partners.
Your work will contribute directly to ensuring that complex biologic processes run smoothly and that therapies can move safely from manufacturing to patients.
A Role at the Center of Modern Biopharmaceutical Production
In this role, you will be closely involved in the daily execution of manufacturing activities in a regulated GMP environment. You will help plan and perform selected steps in the downstream production process while ensuring that documentation and procedures are followed with the highest level of accuracy.
A typical week may involve preparing buffers according to defined recipes, supporting purification activities, and documenting production steps in batch records. You will collaborate with colleagues across the production organization to ensure smooth operations and reliable delivery of material to the next stages of manufacturing.
Beyond daily operations, you will contribute to continuous improvement initiatives and support troubleshooting of production challenges together with colleagues from QA, QC, Process Engineering, and Manufacturing Product Support. You will also participate in onboarding new technicians while continuing to build your own technical expertise in downstream processing.
A Team Built on Collaboration and Professional Pride
You will join a team of technicians and scientists who work in a professional and supportive environment where collaboration and accountability are key.
The team works closely with colleagues across the organization and shares a strong commitment to quality, safety, and compliance. Knowledge sharing is part of everyday work, and employees are encouraged to contribute ideas that improve processes and strengthen production performance.
Working in SYD22 also means being part of an exciting facility ramp-up, where new processes, technologies, and ways of working are continuously being implemented.
What Will Help You Succeed
We are looking for someone who enjoys working in a structured and quality-focused manufacturing environment and who takes pride in contributing to reliable production.
You likely have:
Experience with LEAN, 5S, or continuous improvement initiatives will be considered an advantage.
Just as important, you are someone who approaches new tasks with curiosity, takes responsibility for your work, and contributes positively to the team environment.
A Global Biotech Environment with Real Opportunities
AGC Biologics is a global Contract Development and Manufacturing Organization (CDMO) supporting biotech and pharmaceutical companies in bringing new biologic medicines to patients around the world.
In Søborg, you will work in an international production environment with modern technologies, experienced colleagues, and strong cross-functional collaboration. We focus on developing our people and creating opportunities to grow both technically and professionally while contributing to meaningful work.
Join Our Team
The position follows a shift-based schedule supporting 24/7 production, including weekends and holidays depending on your assigned shifts.
If you are motivated by working in a dynamic GMP manufacturing environment and want to help produce biologic medicines for patients worldwide, we would love to hear from you.
Please submit your application through our recruitment system. Applications will be reviewed continuously.
To support an inclusive recruitment process, we kindly ask candidates not to include a photo in their CV.
Our culture at AGC Biologics is defined by the six core values: Knowledge, Trust, Quality, Ingenuity, Accountability and Teamwork. Our core values stem from our team members and are embedded into our DNA. They provide a common language and understanding of how we as an organization are connected across three continents. Our core values serve as a compass and reminder of how we achieve our purpose of bringing hope to life for patients around the globe.
AGC Biologics is a leading global biopharmaceutical Contract Development and Manufacturing Organization (CDMO) with a strong commitment to delivering the highest standard of service as we work side-by-side with our clients and partners, every step of the way. We provide world-class development and manufacture of mammalian and microbial-based therapeutic proteins, plasmid DNA (pDNA), messenger RNA (mRNA), viral vectors, and genetically engineered cells. Our global network spans the U.S., Europe, and Asia, with cGMP-compliant facilities in Seattle, Washington; Boulder and Longmont, Colorado; Copenhagen, Denmark; Heidelberg, Germany; Milan, Italy; and Chiba, Japan. We currently employ more than 2,500 employees worldwide. Our commitment to continuous innovation fosters the technical creativity to solve our clients’ most complex challenges, including specialization in fast-track projects and rare diseases. AGC Biologics is the partner of choice. To learn more, visit www.agcbio.com. Want to keep posted about our growth and learn more about our company? Follow us on LinkedIn and give us a quick Like on Facebook!
AGC Biologics offers a highly competitive compensation package and a friendly, collaborative culture that values personal initiative and professional achievement. AGC Biologics is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, color, family or medical care leave, gender identity or expression, genetic information, marital status, medical condition, national origin, physical or mental disability, political affiliation, protected veteran status, race, religion, sexual orientation, or any other characteristic protected by applicable laws, regulations and ordinances.